The challenge of high temperatures in deep mining remains harmful to the health of workers and their production efficiency The addition of phase change materials (PCMs) to filling slurry and the use of the cold storag...The challenge of high temperatures in deep mining remains harmful to the health of workers and their production efficiency The addition of phase change materials (PCMs) to filling slurry and the use of the cold storage function of these materials to reduce downhole temperatures is an effective approach to alleviate the aforementioned problem.Paraffin–CaCl_(2)·6H_(2)O composite PCM was prepared in the laboratory.The composition,phase change latent heat,thermal conductivity,and cemented tailing backfill (CTB) compressive strength of the new material were studied.The heat transfer characteristics and endothermic effect of the PCM were simulated using Fluent software.The results showed the following:(1) The new paraffin–CaCl_(2)·6H_(2)O composite PCM improved the thermal conductivity of native paraffin while avoiding the water solubility of CaCl_(2)·6H_(2)O.(2) The calculation formula of the thermal conductivity of CaCl_(2)·6H_(2)O combined with paraffin was deduced,and the reasons were explained in principle.(3) The“enthalpy–mass scale model”was applied to calculate the phase change latent heat of nonreactive composite PCMs.(4)The addition of the paraffin–CaCl_(2)·6H_(2)O composite PCM reduced the CTB strength but increased its heat absorption capacity.This research can give a theoretical foundation for the use of heat storage backfill in green mines.展开更多
CaCl_(2)·6H_(2)O/expanded vermiculite shape stabilized phase change materials(CEV)was prepared by atmospheric impregnation method.Using gold mine tailings as aggregate of cemented paste backfill(CPB)material,the ...CaCl_(2)·6H_(2)O/expanded vermiculite shape stabilized phase change materials(CEV)was prepared by atmospheric impregnation method.Using gold mine tailings as aggregate of cemented paste backfill(CPB)material,the CPB with CEV added was prepared,and the specific heat capacity,thermal conductivity,and uniaxial compressive strength(UCS)of CPB with different cement-tailing ratios and CEV addition ratios were tested,the influence of the above variables on the thermal and mechanical properties of CPB was analyzed.The results show that the maximum encapsulation capacity of expanded vermiculite for CaCl_(2)·6H_(2)O is about 60%,and the melting and solidification enthalpies of CEV can reach 98.87 J/g and 97.56 J/g,respectively.For the CPB without CEV,the specific heat capacity,thermal conductivity,and UCS decrease with the decrease of cement-tailing ratio.For the CPB with CEV added,with the increase of CEV addition ratio,the specific heat capacity increases significantly,and the sensible heat storage capacity and latent heat storage capacity can be increased by at least 10.74%and 218.97%respectively after adding 12%CEV.However,the addition of CEV leads to the increase of pores,and the thermal conductivity and UCS both decrease with the increase of CEV addition.When cement-tailing ratio is 1:8 and 6%,9%,and 12%of CEV are added,the 28-days UCS of CPB is less than 1 MPa.Considering the heat storage capacity and cost price of backfill,the recommended proportion scheme of CPB material presents cement-tailing ratio of 1:6 and 12%CEV,and the most recommended heat storage/release temperature cycle range of CPB with added CEV is from 20 to 40℃.This work can provide theoretical basis for the utilization of heat storage backfill in green mines.展开更多
In this work,a new(Y,Gd)H_(2) precipitate was identified and systematically investigated in the as-cast Mg-6Gd-3Y-0.5Zr alloy by XRD,SEM with EDS,TEM with EDS techniques and thermodynamics analysis.Results show that t...In this work,a new(Y,Gd)H_(2) precipitate was identified and systematically investigated in the as-cast Mg-6Gd-3Y-0.5Zr alloy by XRD,SEM with EDS,TEM with EDS techniques and thermodynamics analysis.Results show that the as-cast alloy contains α-Mg,Mg_(24)(Gd,Y)_(5),and(Y,Gd)H_(2) phase.The(Y,Gd)H_(2) phase usually forms near the eutectic phase Mg_(24)(Gd,Y)_(5) or in the α-Mg grains,displaying a rectangle-shape.The Mg_(24)(Gd,Y)_(5) and(Y,Gd)H_(2) phases crystalize in bcc and fcc structure,respectively,and the(Y,Gd)H_(2) phase has a semi-coherent relationship with α-Mg matrix.The thermodynamics calculation results reveal that the hydrogen dissolved in the melt leads to the formation of hydrides.It is also found that the(Y,Gd)H_(2) hydride can form directly from the liquid phase during solidification.Additionally,it can precipitate by the decomposition of Mg_(24)(Gd,Y)_(5) phase due to absorbing hydrogen from the remaining melt.展开更多
Investigation of the substitution process can provide a better understanding of the superconducting mechanisms in cuprous oxide materials. In this work the effects of substitution Lanthanum (La) for Gadolinium (Gd) on...Investigation of the substitution process can provide a better understanding of the superconducting mechanisms in cuprous oxide materials. In this work the effects of substitution Lanthanum (La) for Gadolinium (Gd) on the structure and oxygen content for x = 0.0 - 0.5 in the compound Gd1-xLaxBa2Cu3O7-δ (GLBCO-123 phase) have been investigated. Samples were synthesized by using a wet-mixing method from powders of Gd2O2, La2O2, BaO, CuO, and solution of HNO3. Based on the analysis of XRD data and SEM-EDXA, it confirms that the sample has formed the GLBCO-123 phase, as expected. It has been obtained that the lattice parameters a and c are increased while the parameter b is slightly decreased with increasing content of Lanthanum. The oxygen content slightly decreased and structure of the Gd1-xLaxBa2Cu3O7-δ phase changed from orthorhombic to tetragonal with increasing the content of Lanthanum.展开更多
In this work,to study the phase structure effect,three groups of Cu/REO catalysts were prepared with cubic and monoclinic Gd_(2)O_(3),Eu_(2)O_(3)and Sm_(2)O_(3) supports for MSR reaction to produce H_(2).Based on CH3O...In this work,to study the phase structure effect,three groups of Cu/REO catalysts were prepared with cubic and monoclinic Gd_(2)O_(3),Eu_(2)O_(3)and Sm_(2)O_(3) supports for MSR reaction to produce H_(2).Based on CH3OH conversion and H_(2)yield,the reaction perfo rmance of the catalysts ranks as Cu/Sm_(2)O_(3)-M>Cu/Sm_(2)O_(3)-C>Cu/Gd_(2)O_(3)-M>Cu/Gd_(2)O_(3)-C>Cu/Eu_(2)O_(3)-M>Cu/Eu_(2)O_(3)-C.For the same kind of REO,Cu supported on the monoclinic support shows better performance than on the cubic one.Despite the phase structure difference,Sm_(2)O_(3) is the best support among all the three kinds of REOs.Compared with Cu/REO catalysts prepared with cubic supports,the corresponding catalysts prepared with monoclinic supports generally possess mo re surface oxygen vacancies,which can generate mo re surface active oxygen(O_(2)^(-)) and moderate basic sites.Moreover,the contents of Cu^(+) on the catalysts follow the same sequence.The reaction performance is positively related to the amount of these three types of surface sites.But metallic Cuo species is necessary to maintain the Cu^(+)■Cu^(0) redox cycle.Furthe rmore,on a catalyst with good perfo rmance,those vital surface reaction intermediates can be stabilized during the reaction.Cu/Sm_(2)O_(3)-M possesses the largest quantities of these surface sites,and has the appropriate amount of Cu^(+) and Cu^(0) after reduction,thereby displaying the optimal performance in all the catalysts.In conclusion,evident support crystal structure effect is observed for Cu/REO catalysts,and a monoclinic phase REO is a better support than the respective cubic phase one.展开更多
As one of the 2D transition metal sulfides,1T phase MoS_(2) nanosheets(NSs)have been studied because of their distinguished conductivity and suitable electronic structure.Nevertheless,the active sites are limited to a...As one of the 2D transition metal sulfides,1T phase MoS_(2) nanosheets(NSs)have been studied because of their distinguished conductivity and suitable electronic structure.Nevertheless,the active sites are limited to a small number of edge sites only,while the basal plane is catalytically inert.Herein,we report that boron(B)doped 1T phase MoS_(2) NSs can replace precious metals as a co-catalyst to assist in photocatalytic H_(2) production of 2D layered g-C_(3)N_(4) nanosheets(g-C_(3)N_(4) NSs).The H_(2) evolution rate of prepared B-MoS_(2)@g-C_(3)N_(4) composites with 15 wt%B-MoS_(2)(B-MoS_(2)@g-C_(3)N_(4)–15,1612.75μmol h^(−1) g^(−1))is 52.33 times of pure g-C_(3)N_(4) NSs(30.82μmol h^(−1) g^(−1)).Furthermore,the apparent quantum efficiency(AQE)of B-MoS_(2)@g-C_(3)N_(4)–15 composites under the light atλ=370 nm is calculated and reaches 5.54%.The excellent photocatalytic performance of B-MoS_(2)@g-C_(3)N_(4)–15 composites is attributed to the B ions doping inducing the distortion of 1T phase MoS_(2) crystal,which can activate more base planes to offer more active sites for H_(2) evolution reaction(HER).This work of B-MoS_(2)@g-C_(3)N_(4) composites offers experience in the progress of effective and low-price photocatalysts for HER.展开更多
基金financial support provided by the National Natural Science Foundation of China (No. 52174106)the Key Technology Research and Development Program (No. 2022YFC2905102)。
文摘The challenge of high temperatures in deep mining remains harmful to the health of workers and their production efficiency The addition of phase change materials (PCMs) to filling slurry and the use of the cold storage function of these materials to reduce downhole temperatures is an effective approach to alleviate the aforementioned problem.Paraffin–CaCl_(2)·6H_(2)O composite PCM was prepared in the laboratory.The composition,phase change latent heat,thermal conductivity,and cemented tailing backfill (CTB) compressive strength of the new material were studied.The heat transfer characteristics and endothermic effect of the PCM were simulated using Fluent software.The results showed the following:(1) The new paraffin–CaCl_(2)·6H_(2)O composite PCM improved the thermal conductivity of native paraffin while avoiding the water solubility of CaCl_(2)·6H_(2)O.(2) The calculation formula of the thermal conductivity of CaCl_(2)·6H_(2)O combined with paraffin was deduced,and the reasons were explained in principle.(3) The“enthalpy–mass scale model”was applied to calculate the phase change latent heat of nonreactive composite PCMs.(4)The addition of the paraffin–CaCl_(2)·6H_(2)O composite PCM reduced the CTB strength but increased its heat absorption capacity.This research can give a theoretical foundation for the use of heat storage backfill in green mines.
基金supported by the National Natural Science Foundation of China(Nos.51974225,51874229,51674188,51904224,51904225)the Shaanxi Innovative Talents Cultivate Program-New-star Plan of Science and Technology,China(No.2018KJXX-083)+2 种基金the Natural Science Basic Research Plan of Shaanxi Province of China(Nos.2018JM 5161,2018JQ5183,2019JM-074)the Scientific Research Program funded by the Shaanxi Provincial Education Department,China(No.19JK0543)the Outstanding Youth Science Fund of Xi’an University of Science and Technology,China(No.2018YQ2-01)。
文摘CaCl_(2)·6H_(2)O/expanded vermiculite shape stabilized phase change materials(CEV)was prepared by atmospheric impregnation method.Using gold mine tailings as aggregate of cemented paste backfill(CPB)material,the CPB with CEV added was prepared,and the specific heat capacity,thermal conductivity,and uniaxial compressive strength(UCS)of CPB with different cement-tailing ratios and CEV addition ratios were tested,the influence of the above variables on the thermal and mechanical properties of CPB was analyzed.The results show that the maximum encapsulation capacity of expanded vermiculite for CaCl_(2)·6H_(2)O is about 60%,and the melting and solidification enthalpies of CEV can reach 98.87 J/g and 97.56 J/g,respectively.For the CPB without CEV,the specific heat capacity,thermal conductivity,and UCS decrease with the decrease of cement-tailing ratio.For the CPB with CEV added,with the increase of CEV addition ratio,the specific heat capacity increases significantly,and the sensible heat storage capacity and latent heat storage capacity can be increased by at least 10.74%and 218.97%respectively after adding 12%CEV.However,the addition of CEV leads to the increase of pores,and the thermal conductivity and UCS both decrease with the increase of CEV addition.When cement-tailing ratio is 1:8 and 6%,9%,and 12%of CEV are added,the 28-days UCS of CPB is less than 1 MPa.Considering the heat storage capacity and cost price of backfill,the recommended proportion scheme of CPB material presents cement-tailing ratio of 1:6 and 12%CEV,and the most recommended heat storage/release temperature cycle range of CPB with added CEV is from 20 to 40℃.This work can provide theoretical basis for the utilization of heat storage backfill in green mines.
基金financially supported by the Key Project of Equipment Pre-research Field Fund under Grant No.61409230407the National Natural Science Foundation of China(NSFC)under Grant No.51601054the Central Government Guides Local Science and Technology Development Fund Projects under Grant No.206Z1005G。
文摘In this work,a new(Y,Gd)H_(2) precipitate was identified and systematically investigated in the as-cast Mg-6Gd-3Y-0.5Zr alloy by XRD,SEM with EDS,TEM with EDS techniques and thermodynamics analysis.Results show that the as-cast alloy contains α-Mg,Mg_(24)(Gd,Y)_(5),and(Y,Gd)H_(2) phase.The(Y,Gd)H_(2) phase usually forms near the eutectic phase Mg_(24)(Gd,Y)_(5) or in the α-Mg grains,displaying a rectangle-shape.The Mg_(24)(Gd,Y)_(5) and(Y,Gd)H_(2) phases crystalize in bcc and fcc structure,respectively,and the(Y,Gd)H_(2) phase has a semi-coherent relationship with α-Mg matrix.The thermodynamics calculation results reveal that the hydrogen dissolved in the melt leads to the formation of hydrides.It is also found that the(Y,Gd)H_(2) hydride can form directly from the liquid phase during solidification.Additionally,it can precipitate by the decomposition of Mg_(24)(Gd,Y)_(5) phase due to absorbing hydrogen from the remaining melt.
文摘Investigation of the substitution process can provide a better understanding of the superconducting mechanisms in cuprous oxide materials. In this work the effects of substitution Lanthanum (La) for Gadolinium (Gd) on the structure and oxygen content for x = 0.0 - 0.5 in the compound Gd1-xLaxBa2Cu3O7-δ (GLBCO-123 phase) have been investigated. Samples were synthesized by using a wet-mixing method from powders of Gd2O2, La2O2, BaO, CuO, and solution of HNO3. Based on the analysis of XRD data and SEM-EDXA, it confirms that the sample has formed the GLBCO-123 phase, as expected. It has been obtained that the lattice parameters a and c are increased while the parameter b is slightly decreased with increasing content of Lanthanum. The oxygen content slightly decreased and structure of the Gd1-xLaxBa2Cu3O7-δ phase changed from orthorhombic to tetragonal with increasing the content of Lanthanum.
基金Project supported by the National Natural Science Foundation of China(22172071,22102069,22062013,22262021,21962009)Natural Science Foundation of Jiangxi Province,China(20202BAB203006,20212BAB203030)Key Laboratory Foundation of Jiangxi Province for Environment and Energy Catalysis,China(20181BCD40004).
文摘In this work,to study the phase structure effect,three groups of Cu/REO catalysts were prepared with cubic and monoclinic Gd_(2)O_(3),Eu_(2)O_(3)and Sm_(2)O_(3) supports for MSR reaction to produce H_(2).Based on CH3OH conversion and H_(2)yield,the reaction perfo rmance of the catalysts ranks as Cu/Sm_(2)O_(3)-M>Cu/Sm_(2)O_(3)-C>Cu/Gd_(2)O_(3)-M>Cu/Gd_(2)O_(3)-C>Cu/Eu_(2)O_(3)-M>Cu/Eu_(2)O_(3)-C.For the same kind of REO,Cu supported on the monoclinic support shows better performance than on the cubic one.Despite the phase structure difference,Sm_(2)O_(3) is the best support among all the three kinds of REOs.Compared with Cu/REO catalysts prepared with cubic supports,the corresponding catalysts prepared with monoclinic supports generally possess mo re surface oxygen vacancies,which can generate mo re surface active oxygen(O_(2)^(-)) and moderate basic sites.Moreover,the contents of Cu^(+) on the catalysts follow the same sequence.The reaction performance is positively related to the amount of these three types of surface sites.But metallic Cuo species is necessary to maintain the Cu^(+)■Cu^(0) redox cycle.Furthe rmore,on a catalyst with good perfo rmance,those vital surface reaction intermediates can be stabilized during the reaction.Cu/Sm_(2)O_(3)-M possesses the largest quantities of these surface sites,and has the appropriate amount of Cu^(+) and Cu^(0) after reduction,thereby displaying the optimal performance in all the catalysts.In conclusion,evident support crystal structure effect is observed for Cu/REO catalysts,and a monoclinic phase REO is a better support than the respective cubic phase one.
基金fundings from the National Natural Science Foundation of China(No.51872173)Taishan Scholars Program of Shandong Province(No.tsqn201812068)+1 种基金Natural Science Foundation of Shandong Province(No.ZR2022JQ21)Higher School Youth Innovation Team of Shandong Province(No.2019KJA013).
文摘As one of the 2D transition metal sulfides,1T phase MoS_(2) nanosheets(NSs)have been studied because of their distinguished conductivity and suitable electronic structure.Nevertheless,the active sites are limited to a small number of edge sites only,while the basal plane is catalytically inert.Herein,we report that boron(B)doped 1T phase MoS_(2) NSs can replace precious metals as a co-catalyst to assist in photocatalytic H_(2) production of 2D layered g-C_(3)N_(4) nanosheets(g-C_(3)N_(4) NSs).The H_(2) evolution rate of prepared B-MoS_(2)@g-C_(3)N_(4) composites with 15 wt%B-MoS_(2)(B-MoS_(2)@g-C_(3)N_(4)–15,1612.75μmol h^(−1) g^(−1))is 52.33 times of pure g-C_(3)N_(4) NSs(30.82μmol h^(−1) g^(−1)).Furthermore,the apparent quantum efficiency(AQE)of B-MoS_(2)@g-C_(3)N_(4)–15 composites under the light atλ=370 nm is calculated and reaches 5.54%.The excellent photocatalytic performance of B-MoS_(2)@g-C_(3)N_(4)–15 composites is attributed to the B ions doping inducing the distortion of 1T phase MoS_(2) crystal,which can activate more base planes to offer more active sites for H_(2) evolution reaction(HER).This work of B-MoS_(2)@g-C_(3)N_(4) composites offers experience in the progress of effective and low-price photocatalysts for HER.